JP5819410B2 - Fiber, non-woven fabric and its use - Google Patents

Fiber, non-woven fabric and its use Download PDF

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Publication number
JP5819410B2
JP5819410B2 JP2013512354A JP2013512354A JP5819410B2 JP 5819410 B2 JP5819410 B2 JP 5819410B2 JP 2013512354 A JP2013512354 A JP 2013512354A JP 2013512354 A JP2013512354 A JP 2013512354A JP 5819410 B2 JP5819410 B2 JP 5819410B2
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fiber
nonwoven fabric
weight
acid
anionic surfactant
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JPWO2012147694A1 (en
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富田 嘉彦
嘉彦 富田
鈴木 健一
健一 鈴木
大亮 菅原
大亮 菅原
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Mitsui Chemicals Inc
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Mitsui Chemicals Inc
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/511Topsheet, i.e. the permeable cover or layer facing the skin
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/44Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/46Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/511Topsheet, i.e. the permeable cover or layer facing the skin
    • A61F13/51113Topsheet, i.e. the permeable cover or layer facing the skin comprising an additive, e.g. lotion or odour control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/511Topsheet, i.e. the permeable cover or layer facing the skin
    • A61F13/51121Topsheet, i.e. the permeable cover or layer facing the skin characterised by the material
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282Addition polymers
    • D04H1/4291Olefin series
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/005Synthetic yarns or filaments
    • D04H3/007Addition polymers
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2509/00Medical; Hygiene
    • D10B2509/02Bandages, dressings or absorbent pads
    • D10B2509/026Absorbent pads; Tampons; Laundry; Towels
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60Nonwoven fabric [i.e., nonwoven strand or fiber material]

Description

本発明は、有害菌の増殖が抑制され、皮膚のかぶれが低減される、紙おむつ、生理用品などの衛生材料のトップシート等に好適な繊維、かかる繊維を含む不織布に関する。   The present invention relates to a fiber suitable for a top sheet of sanitary materials such as disposable diapers and sanitary products, in which growth of harmful bacteria is suppressed and skin irritation is reduced, and a nonwoven fabric including such a fiber.

ポリプロピレンに代表されるオレフィン系重合体から得られる不織布は通気性、柔軟性、軽量性に優れることから衛生材料を始めとする各種用途に幅広く用いられている。そのため、不織布には、その用途に応じた各種の特性が求められるとともに、その特性の向上が要求されている。   Nonwoven fabrics obtained from olefin polymers typified by polypropylene are widely used in various applications including sanitary materials because of their excellent breathability, flexibility and lightness. For this reason, the nonwoven fabric is required to have various properties according to its use and to improve the properties.

例えば、紙おむつなどの衛生材料として用いる場合、肌にやさしい柔軟性、すばやく尿を移行できる吸収性、蒸れを防ぐための通気性、菌等による皮膚のかぶれ、悪臭の発生を防ぐための抗菌性が不織布に求められる。特に、皮膚のかぶれは利用者にとって大きな負担となることから、かぶれの因子となる菌や悪臭の発生を抑えるための方法が種々検討されている。特に近年、皮膚が弱酸性であることから、皮膚環境を弱酸性にすることで皮膚に有益な菌の増殖を助け、その結果、皮膚に有害な菌の増殖を抑えることで菌由来の皮膚かぶれが低減できることが明らかとなってきた。   For example, when used as a sanitary material such as paper diapers, it has skin-friendly flexibility, absorbability to quickly transfer urine, breathability to prevent stuffiness, antibacterial properties to prevent skin irritation caused by bacteria, etc. Required for non-woven fabrics. In particular, since skin irritation is a heavy burden on users, various methods for suppressing the generation of bacteria and malodors that cause irritation have been studied. Especially in recent years, since the skin is weakly acidic, by making the skin environment weakly acidic, it helps the growth of bacteria beneficial to the skin, and as a result, the growth of bacteria harmful to the skin is suppressed, resulting in skin irritation from bacteria. It has become clear that can be reduced.

例えば、特表2003−516778号公報(特許文献1)には、不織布にクエン酸またはクエン酸ナトリウムからなるpH制御材を含浸させ、接触する皮膚のpHと同程度のpH環境を保つ方法が開示されている。しかしながら、特許文献1に記載されているクエン酸は水溶性であることから、一旦、尿に接触するとクエン酸などのpH制御材が流れ出して吸収体の方へ移行してしまうため、pHの維持は困難である。また、例えば、特開2004−176225号公報(特許文献2)には、ベタイン型両性化合物、アルキレンオキサイド付加型非イオン界面活性剤及び/又はカルボン酸塩などのアニオン界面活性剤からなる繊維処理剤を付着させた消臭性繊維を用いる方法が開示されている。しかしながら、特許文献2に記載の繊維処理剤は塗布により繊維に付着されていることから、一旦、尿に接触すると繊維処理剤が一部流れ出し、吸収体の方へ移行してしまい、上記特許文献1と同様に効果の維持という点で満足できるものではない。   For example, Japanese translations of PCT publication No. 2003-516778 (patent document 1) discloses a method of impregnating a non-woven fabric with a pH control material made of citric acid or sodium citrate to maintain a pH environment comparable to the pH of the contacting skin. Has been. However, since citric acid described in Patent Document 1 is water-soluble, once it comes into contact with urine, a pH control material such as citric acid flows out and moves toward the absorber. It is difficult. Further, for example, Japanese Patent Application Laid-Open No. 2004-176225 (Patent Document 2) discloses a fiber treatment agent comprising a betaine amphoteric compound, an alkylene oxide addition type nonionic surfactant and / or an anionic surfactant such as a carboxylate. A method using a deodorant fiber to which is attached is disclosed. However, since the fiber treatment agent described in Patent Document 2 is attached to the fibers by coating, once the fiber treatment agent comes into contact with urine, the fiber treatment agent partially flows out and moves toward the absorbent body. Similar to 1, it is not satisfactory in terms of maintaining the effect.

一方、例えば、特表2005−530857号公報(特許文献3)には抗菌活性物質と陰イオン性界面活性剤とを含む抗菌組成物を用いる方法が、特表2002−505918号公報(特許文献4)にはプロトン供与性活性成分を含むスキンケア組成物を用いる方法など、種々の方法が提案されている。しかしながら、いずれの方法でも経時で効果が低減してしまうという問題がある。また、抗菌組成物を用いる方法においては、抗菌剤作用により一時的に菌の増殖を低減できるが、有害な菌と共に有益な菌の増殖も抑えられてしまうために、かえって有害菌の増殖を招くこととなる。従って、先行技術においては、おむつ着用時に発生する皮膚のかぶれを抑制する効果は不十分であり、さらなる改良が求められている。   On the other hand, for example, Japanese Patent Publication No. 2005-530857 (Patent Document 3) discloses a method using an antibacterial composition containing an antibacterial active substance and an anionic surfactant. Various methods such as a method using a skin care composition containing a proton-donating active ingredient have been proposed. However, any method has a problem that the effect is reduced with time. In addition, in the method using an antibacterial composition, the growth of bacteria can be temporarily reduced by the action of an antibacterial agent, but the growth of beneficial bacteria together with harmful bacteria is also suppressed. It will be. Therefore, in the prior art, the effect of suppressing skin irritation that occurs when a diaper is worn is insufficient, and further improvement is required.

特表2003−516778号公報Special table 2003-516778 gazette 特開2004−176225号公報JP 2004-176225 A 特表2005−530857号公報JP 2005-530857 A 特表2002−505918号公報Japanese translation of PCT publication No. 2002-505918

本発明者らは、有害菌の増殖が抑制され、皮膚のかぶれの抑制を持続させることが可能な紙おむつ、生理用品などの衛生材料のトップシート、あるいはセカンドシートに好適な繊維、かかる繊維を含む不織布を開発することを目的として検討を行った結果、酸形態のアニオン系界面活性剤を含むオレフィン系重合体組成物より得られる繊維、かかる繊維を含む不織布が前記目的を達成し得ることを見出した。   The present inventors include a fiber suitable for a top sheet of a sanitary material such as a disposable diaper, a sanitary product, or a second sheet in which the growth of harmful bacteria is suppressed and the suppression of skin irritation can be sustained. As a result of studies conducted for the purpose of developing a nonwoven fabric, it has been found that a fiber obtained from an olefin polymer composition containing an anionic surfactant in an acid form, and a nonwoven fabric containing such a fiber can achieve the object. It was.

本発明は、オレフィン系重合体100重量部に対して、酸形態のアニオン系界面活性剤を0.1〜30重量部含むオレフィン系重合体組成物からなる繊維であって、前記酸形態のアニオン系界面活性剤が、繊維に溶融混錬されてなる繊維を提供するものである。   The present invention is a fiber comprising an olefin polymer composition containing 0.1 to 30 parts by weight of an anionic surfactant in an acid form with respect to 100 parts by weight of an olefin polymer, the anion in the acid form The system surfactant provides a fiber obtained by melt-kneading the fiber.

本発明に係る繊維、および当該繊維を含む不織布は、おむつなどの衛生材料として使用した場合に、有害菌の増殖が抑制され、皮膚のかぶれの抑制効果の持続性が高いという特徴を有する。   When used as a sanitary material such as diapers, the fiber according to the present invention and the nonwoven fabric containing the fiber are characterized in that the growth of harmful bacteria is suppressed and the sustainability of the skin irritation suppression effect is high.

<オレフィン系重合体>
本発明の繊維及び当該繊維を含む不織布を形成するオレフィン系重合体は、エチレン、プロピレン、1−ブテン、1−ヘキセン、4−メチル−1−ペンテン及び1−オクテン等のα−オレフィンの単独若しくは共重合体であり、具体的には、高圧法低密度ポリエチレン、線状低密度ポリエチレン(所謂LLDPE)、高密度ポリエチレン、エチレン・プロピレンランダム共重合体、エチレン・1−ブテンランダム共重合体等のエチレンの単独重合体あるいはエチレン・α−オレフィン共重合体等のエチレン系重合体;プロピレンの単独重合体(所謂ポリプロピレン)、プロピレン・エチレンランダム共重合体、プロピレン・エチレン・1−ブテンランダム共重合体(所謂ランダムポリプロピレン)、プロピレンブロック共重合体、プロピレン・1−ブテンランダム共重合体等のプロピレン系重合体;1−ブテン単独重合体、1−ブテン・エチレン共重合体、1−ブテン・プロピレン共重合体等の1−ブテン系重合体;ポリ4−メチル−1−ペンテン等が挙げられる。
<Olefin polymer>
The olefin polymer forming the fiber of the present invention and the nonwoven fabric containing the fiber is an α-olefin such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene alone or Specifically, high pressure method low density polyethylene, linear low density polyethylene (so-called LLDPE), high density polyethylene, ethylene / propylene random copolymer, ethylene / 1-butene random copolymer, etc. Ethylene polymers such as ethylene homopolymers or ethylene / α-olefin copolymers; propylene homopolymers (so-called polypropylene), propylene / ethylene random copolymers, propylene / ethylene / 1-butene random copolymers (So-called random polypropylene), propylene block copolymer, propylene Propylene polymers such as 1-butene random copolymer; 1-butene polymers such as 1-butene homopolymer, 1-butene / ethylene copolymer, 1-butene / propylene copolymer; poly-4- And methyl-1-pentene.

これらオレフィン系重合体の中でも、プロピレン系重合体が、成形時の紡糸安定性や不織布の加工性及び通気性、柔軟性、軽量性、耐熱性に優れる不織布が得られるので、好ましい。   Among these olefin polymers, a propylene polymer is preferable because a nonwoven fabric excellent in spinning stability during molding, processability and breathability of the nonwoven fabric, flexibility, light weight, and heat resistance can be obtained.

本発明に係るオレフィン系重合体には、本発明の目的を損なわない範囲で、親水性を促進または抑制する助剤、通常用いられる酸化防止剤、耐候安定剤、耐光安定剤、ブロッキング防止剤、滑剤、核剤、顔料、柔軟剤、撥水剤、フィラー、抗菌剤等の添加剤あるいはオレフィン系重合体以外の重合体を必要に応じて配合することができる。   In the olefin polymer according to the present invention, an auxiliary agent that promotes or suppresses hydrophilicity within a range that does not impair the object of the present invention, a commonly used antioxidant, weathering stabilizer, light stabilizer, antiblocking agent, Additives such as a lubricant, a nucleating agent, a pigment, a softening agent, a water repellent, a filler, an antibacterial agent, or a polymer other than an olefin polymer can be blended as necessary.

<プロピレン系重合体>
本発明に係わるプロピレン系重合体としては、通常、融点(Tm)が125℃以上、好ましくは130〜165℃の範囲にあるプロピレンの単独重合体若しくはプロピレンと少量のエチレン、1−ブテン、1−ペンテン、1−ヘキセン、1−オクテン、4−メチル−1−ペンテン等の炭素数2以上(但し炭素数3を除く)、好ましくは2〜8(但し炭素数3を除く)の1種または2種以上のα−オレフィンとの共重合体が好ましい。
<Propylene polymer>
The propylene polymer according to the present invention is usually a propylene homopolymer having a melting point (Tm) of 125 ° C. or higher, preferably 130 to 165 ° C., or a small amount of ethylene, 1-butene, 1- One or two of 2 or more carbon atoms (excluding 3 carbon atoms), preferably 2-8 (excluding 3 carbon atoms) such as pentene, 1-hexene, 1-octene, 4-methyl-1-pentene Copolymers with more than one α-olefin are preferred.

本発明に係わるプロピレン系重合体は、溶融紡糸し得る限り、メルトフローレート(MFR:ASTMD−1238、230℃、荷重2160g)は特に限定はされないが、通常、1〜1000g/10分、好ましくは5〜500g/10分、さらに好ましくは10〜100g/10分の範囲にある。   As long as the propylene polymer according to the present invention can be melt-spun, the melt flow rate (MFR: ASTM D-1238, 230 ° C., load 2160 g) is not particularly limited, but is usually 1 to 1000 g / 10 minutes, preferably It is in the range of 5 to 500 g / 10 minutes, more preferably 10 to 100 g / 10 minutes.

本発明に係わるプロピレン系重合体の中でも、融点(Tm)が125〜155℃、好ましくは130〜147℃の範囲にあるプロピレンと少量のエチレン、1−ブテン、1−ペンテン、1−ヘキセン、1−オクテン、4−メチル−1−ペンテン等の炭素数2以上、好ましくは2〜8の1種または2種以上のα−オレフィンとのプロピレン・α−オレフィンランダム共重合体が、柔軟性、初期親水性に優れる不織布が得られるので、とくに好ましい。   Among the propylene polymers according to the present invention, propylene and a small amount of ethylene, 1-butene, 1-pentene, 1-hexene, having a melting point (Tm) in the range of 125 to 155 ° C, preferably 130 to 147 ° C, -Propylene / α-olefin random copolymer with 2 or more carbon atoms, preferably 2 to 8 or more α-olefins such as octene and 4-methyl-1-pentene is flexible, initial This is particularly preferable because a nonwoven fabric having excellent hydrophilicity can be obtained.

プロピレン・α−オレフィンランダム共重合体におけるα−オレフィンの含有量は、融点(Tm)が上記範囲にある限り、特に限定はされないが、通常1〜10モル%の範囲にある。より好ましくは1〜5モル%である。   The α-olefin content in the propylene / α-olefin random copolymer is not particularly limited as long as the melting point (Tm) is in the above range, but is usually in the range of 1 to 10 mol%. More preferably, it is 1-5 mol%.

<酸形態のアニオン系界面活性剤>
本発明に係わる酸形態のアニオン系界面活性剤とは、水あるいは水分の存在下において、酸性を示すことができるアニオン系界面活性剤である。酸形態のアニオン系界面活性剤としては、特に、緩衝能を有することでpHの変化を緩和する能力を発現できることから、弱酸性を示す酸形態のアニオン系界面活性剤が好ましく、具体的には、脂肪酸、或いは酸形態のリン酸エステル型界面活性剤が好ましい。また、酸形態の当該界面活性剤であれば、完全中和塩でない、例えばモノアルキルリン酸エステル塩のような部分中和塩であっても良い。
<Anionic surfactant in acid form>
The anionic surfactant in the acid form according to the present invention is an anionic surfactant that can exhibit acidity in the presence of water or moisture. As the acid form anionic surfactant, an acid form anionic surfactant exhibiting weak acidity is preferable because it can express the ability to alleviate the change in pH by having a buffering ability. , Fatty acid or acid form phosphate ester type surfactants are preferred. Moreover, if it is the said surfactant of an acid form, it may be a partially neutralized salt like a monoalkyl phosphate ester salt which is not a completely neutralized salt.

本発明に係る酸形態のアニオン系界面活性剤としては、通常、疎水性基の炭素数が8以上、より良好な溶融混練性、および押出成型時の安定した運転性を得る観点から好ましくは9以上、より好ましくは12以上、さらに好ましくは13以上の脂肪族炭化水素基を有するアニオン系界面活性剤、特に好ましくは炭素数が18〜28の範囲にある脂肪族炭化水素基を有するアニオン系界面活性剤、あるいは、好ましくは、炭素数が9以上の脂肪酸、好ましくは炭素数が12以上、さらに好ましくは炭素数が13以上、特に好ましくは炭素数が18〜28の範囲にある脂肪酸、もしくは、好ましくは疎水性基の炭素数が9以上のリン酸エステル型界面活性剤、さらに好ましくは疎水性基の炭素数が12以上、さらに好ましくは13以上、特に好ましくは18〜28の範囲にあるリン酸エステル型界面活性剤である。リン酸エステル型界面活性剤としては、脂肪族アルコールとリン酸とのエステルであるアルキルリン酸エステル、脂肪族アルコールのアルキレンオキサイド付加物とリン酸とのエステルであるアルキルエーテルリン酸エステル、芳香族アルコールのアルキレンオキサイド付加物とリン酸とのエステルであるアルキルフェニルエーテルリン酸エステル等が挙げられる。   The anionic surfactant in the acid form according to the present invention is preferably 9 from the viewpoint of usually having a hydrophobic group having 8 or more carbon atoms, better melt-kneading properties, and stable operability during extrusion molding. More preferably, an anionic surfactant having an aliphatic hydrocarbon group having 12 or more, more preferably 13 or more, particularly preferably an anionic interface having an aliphatic hydrocarbon group having 18 to 28 carbon atoms. An activator or, preferably, a fatty acid having 9 or more carbon atoms, preferably 12 or more carbon atoms, more preferably 13 or more carbon atoms, particularly preferably 18 to 28 carbon atoms, or Preferably, the phosphoric acid ester type surfactant has 9 or more carbon atoms in the hydrophobic group, more preferably 12 or more, more preferably 13 or more, particularly preferably the hydrophobic group has 12 or more carbon atoms. Ku is a phosphate ester type surfactant in the range of 18-28. Phosphate-type surfactants include alkyl phosphate esters that are esters of aliphatic alcohols and phosphoric acid, alkyl ether phosphate esters that are esters of aliphatic alcohol alkylene oxide adducts and phosphoric acid, aromatics Examples thereof include alkylphenyl ether phosphates which are esters of an alkylene oxide adduct of alcohol and phosphoric acid.

また、本発明に係る酸形態のアニオン系界面活性剤としては、これらの混合物であってもよい。例えば、炭素数が18〜28の脂肪酸、あるいは、酸形態のリン酸エステル型界面活性剤が、炭素数が18〜28の脂肪族アルコールとリン酸とのエステルであるアルキルリン酸エステル、あるいは炭素数が18〜28の脂肪族アルコールのアルキレンオキサイド付加物とリン酸とのエステルであるアルキルエーテルリン酸エステル、あるいは炭素数が18〜28の芳香族アルコールのアルキレンオキサイド付加物とリン酸とのエステルであるアルキルフェニルエーテルリン酸エステル、或いはそれらの混合物の場合である。炭素数が9以上の脂肪酸、あるいは炭素数が9以上である酸形態のリン酸エステル型界面活性剤、或いはそれらの混合物である場合、より良好な溶融混練性が得られる点、および酸形態のアニオン系界面活性剤が不織布から溶出されることが抑えられ、効果の持続性が得られるので好ましい。   Further, the acid form anionic surfactant according to the present invention may be a mixture thereof. For example, a fatty acid having 18 to 28 carbon atoms, or a phosphoric acid ester type surfactant in an acid form is an alkyl phosphate ester or carbon that is an ester of an aliphatic alcohol having 18 to 28 carbon atoms and phosphoric acid. Alkyl ether phosphoric acid ester which is ester of alkylene oxide adduct of aliphatic alcohol having 18 to 28 and phosphoric acid, or ester of alkylene oxide adduct of aromatic alcohol having 18 to 28 carbon and phosphoric acid In the case of alkyl phenyl ether phosphate ester, or a mixture thereof. In the case of a fatty acid having 9 or more carbon atoms, a phosphate ester type surfactant having 9 or more carbon atoms, or a mixture thereof, a better melt kneadability can be obtained, and It is preferable because the anionic surfactant is suppressed from being eluted from the nonwoven fabric, and the durability of the effect can be obtained.

本発明に係る脂肪酸としては、具体的には、ミリスチン酸、パルミチン酸、ステアリン酸、モンタン酸等の飽和脂肪酸、オレイン酸、リノレン酸、ネルボン酸等の不飽和脂肪酸が挙げられる。   Specific examples of the fatty acid according to the present invention include saturated fatty acids such as myristic acid, palmitic acid, stearic acid, and montanic acid, and unsaturated fatty acids such as oleic acid, linolenic acid, and nervonic acid.

本発明に係る酸形態のリン酸エステル型界面活性剤としては、アルキルリン酸エステルの具体例として、例えば、モノステアリルリン酸エステル、ジステアリルリン酸エステル、モノベヘニルリン酸エステル、ジベヘニルリン酸エステル、モノセチルリン酸エステル、ジセチルリン酸エステル、モノラウリルリン酸エステル、ジラウリルリン酸エステル、モノオクチルリン酸エステル、ジオクチルリン酸エステルなどが、また、アルキルエーテルリン酸エステルの具体例として、例えば、モノ(ポリオキシエチレン・ステアリルエーテル)リン酸エステル、ジ(ポリオキシエチレン・ステアリルエーテル)リン酸エステル、モノ(ポリオキシエチレン・ラウリルエーテル)リン酸エステル、ジ(ポリオキシエチレン・ラウリルエーテル)リン酸エステルなどが、また、アルキルフェニルエーテルリン酸エステルの具体例として、例えば、モノ(ポリオキシエチレン・ステアリルフェニルエーテル)リン酸エステル、ジ(ポリオキシエチレン・ステアリルフェニルエーテル)リン酸エステル、モノ(ポリオキシエチレン・ラウリルフェニルエーテル)リン酸エステル、ジ(ポリオキシエチレン・ラウリルフェニルエーテル)リン酸エステルなどが挙げられる。   As the phosphate ester type surfactant in the acid form according to the present invention, as specific examples of alkyl phosphate esters, for example, monostearyl phosphate ester, distearyl phosphate ester, monobehenyl phosphate ester, dibehenyl phosphate ester, Monocetyl phosphate ester, dicetyl phosphate ester, monolauryl phosphate ester, dilauryl phosphate ester, monooctyl phosphate ester, dioctyl phosphate ester and the like, and specific examples of alkyl ether phosphate ester include, for example, mono (polyoxyethylene・ Stearyl ether) phosphate ester, di (polyoxyethylene stearyl ether) phosphate ester, mono (polyoxyethylene lauryl ether) phosphate ester, di (polyoxyethylene lauryl ether) phosphorus Examples of the alkyl phenyl ether phosphate ester include mono (polyoxyethylene / stearyl phenyl ether) phosphate, di (polyoxyethylene / stearyl phenyl ether) phosphate, mono (poly And oxyethylene / lauryl phenyl ether) phosphate, di (polyoxyethylene / lauryl phenyl ether) phosphate, and the like.

これら酸形態のアニオン系界面活性剤の中でも、特に、酸形態のリン酸エステル型界面活性剤が好ましい。   Among these acid-form anionic surfactants, acid-form phosphate surfactants are particularly preferable.

<ノニオン系界面活性剤>
本発明に係るノニオン系界面活性剤としては、種々公知のノニオン系界面活性剤を使用することが可能であり、それを添加して繊維を形成したときに繊維表面が親水性を呈するものであれば特に限定されない。ノニオン系界面活性剤の具体例としては、脂肪酸グリセライド、アルコキシ化アルキルフェノール、ポリオキシアルキレン脂肪酸エステル、アルキルポリオキシエチレンアルコール、脂肪酸アミド、ポリオキシアルキレンソルビタン脂肪酸エステル、ショ糖脂肪酸エステル、ソルビタン脂肪酸エステル、脂肪酸アルカノールアミド、ポリオキシアルキレンアルキルエーテル、ポリオキシアルキレンアルキルフェニルエーテル、アルキルポリグルコシド、脂肪酸ジエタノールアミド、アルキルモノグリセリルエーテル等が挙げられる。
<Nonionic surfactant>
As the nonionic surfactant according to the present invention, various known nonionic surfactants can be used, and the surface of the fiber exhibits hydrophilicity when added to form a fiber. If it does not specifically limit. Specific examples of nonionic surfactants include fatty acid glycerides, alkoxylated alkylphenols, polyoxyalkylene fatty acid esters, alkyl polyoxyethylene alcohols, fatty acid amides, polyoxyalkylene sorbitan fatty acid esters, sucrose fatty acid esters, sorbitan fatty acid esters, fatty acids Examples include alkanolamides, polyoxyalkylene alkyl ethers, polyoxyalkylene alkyl phenyl ethers, alkyl polyglucosides, fatty acid diethanolamides, and alkyl monoglyceryl ethers.

<オレフィン系重合体組成物>
本発明に係わるオレフィン系重合体組成物は、前記オレフィン系重合体100重量部に対して、前記酸形態のアニオン系界面活性剤を0.1〜30重量部、好ましくは1〜15重量部、さらに好ましくは1.5〜10重量部含む組成物である。
<Olefin polymer composition>
The olefin polymer composition according to the present invention is 0.1 to 30 parts by weight, preferably 1 to 15 parts by weight of the anionic surfactant in the acid form with respect to 100 parts by weight of the olefin polymer. More preferably, the composition contains 1.5 to 10 parts by weight.

酸形態のアニオン系界面活性剤の量が0.1重量部未満では、繊維周辺の環境を弱酸性にする効果が低く、その結果、それを用いた不織布を生理用品、おむつ等の衛生材料に用いた場合には、かぶれ低減効果が不足する虞がある。一方、添加量の上限は特に限定はされないが、30重量部を超えると、繊維周辺の環境を弱酸性にする効果が飽和するともに、得られる繊維及び当該繊維を含む不織布の表面に滲み出す酸形態のアニオン系界面活性剤の量が多くなり、成形加工性が低下する。   If the amount of the anionic surfactant in the acid form is less than 0.1 parts by weight, the effect of making the environment around the fiber weakly acidic is low. As a result, the nonwoven fabric using the fiber is used as a sanitary material such as sanitary goods and diapers. When used, the rash reduction effect may be insufficient. On the other hand, the upper limit of the addition amount is not particularly limited, but if it exceeds 30 parts by weight, the effect of weakening the environment around the fiber is saturated, and the acid that exudes to the surface of the resulting fiber and the nonwoven fabric containing the fiber is saturated. The amount of the anionic surfactant in the form increases, and the molding processability decreases.

本発明に係るオレフィン系重合体組成物は、前記酸形態のアニオン系界面活性剤に加え、更に、前記ノニオン系界面活性剤を前記オレフィン系重合体100重量部に対して、0.1〜30重量部、好ましくは0.5〜15重量部の範囲で含むことにより、得られる繊維の親水性を向上でき、また酸形態のアニオン系界面活性剤による急激なpHの変化を緩和することができる。   In addition to the acid form anionic surfactant, the olefin polymer composition according to the present invention may further include 0.1 to 30 parts of the nonionic surfactant with respect to 100 parts by weight of the olefin polymer. By including in the range of 0.5 parts by weight, preferably 0.5 to 15 parts by weight, the hydrophilicity of the resulting fiber can be improved, and a sudden change in pH due to the acid form anionic surfactant can be mitigated. .

本発明に係るオレフィン系重合体組成物を用意する場合は、前記酸形態のアニオン系界面活性剤を、5重量%を超える、例えば10〜40重量%と高濃度に含むペレット状のマスターバッチとしておくと、繊維及び不織布の製造時に酸形態のアニオン系界面活性剤の添加及び前記オレフィン系重合体との混合が容易となるので好ましい。酸形態のアニオン系界面活性剤との混合物のマスターバッチに用いるオレフィン系重合体は、前記オレフィン系重合体に限らず、他のオレフィン系重合体を用いてもよい。かかるマスターバッチに用いるオレフィン系重合体は目的とする繊維及び当該繊維を含む不織布に応じて、MFRを適宜選択し得る。   When preparing the olefin polymer composition according to the present invention, the anionic surfactant in the acid form is more than 5% by weight, for example, as a pellet-shaped masterbatch containing 10 to 40% by weight in a high concentration. It is preferable to add an anionic surfactant in the acid form and to mix with the olefin polymer at the time of producing fibers and nonwoven fabrics. The olefin polymer used in the master batch of the mixture with the anionic surfactant in the acid form is not limited to the olefin polymer, and other olefin polymers may be used. As the olefin polymer used in such a master batch, MFR can be appropriately selected according to the target fiber and the nonwoven fabric containing the fiber.

本発明に係るオレフィン系重合体組成物には、本発明の目的を損なわない範囲で、通常用いられる酸化防止剤、耐候安定剤、耐光安定剤、ブロッキング防止剤、滑剤、核剤、顔料等の添加剤あるいはオレフィン系重合体以外の重合体を必要に応じて配合することができる。   In the olefin polymer composition according to the present invention, an antioxidant, a weather stabilizer, a light stabilizer, an antiblocking agent, a lubricant, a nucleating agent, a pigment, and the like that are usually used within a range not impairing the object of the present invention. Polymers other than additives or olefin polymers can be blended as required.

<繊維及び不織布>
本発明の繊維及び当該繊維を含む不織布は、前記オレフィン系重合体と前記酸形態のアニオン系界面活性剤及び好ましくは前記ノニオン系界面活性剤を含むオレフィン系重合体組成物の繊維及び当該繊維を含む不織布である。
<Fiber and non-woven fabric>
The fiber of the present invention and the nonwoven fabric containing the fiber include the fiber of the olefin polymer composition containing the olefin polymer and the anionic surfactant in the acid form, and preferably the nonionic surfactant, and the fiber. It is a nonwoven fabric containing.

特に前記オレフィン系重合体に前記酸形態のアニオン系界面活性剤が溶融混錬されてなる場合、皮膚のかぶれを低減する効果が持続するため好ましい。また、前記ノニオン系界面活性剤を併用する場合、前記酸形態のアニオン系界面活性剤と併せて溶融混錬することで、溶融混練性が向上し、前記ノニオン系界面活性剤と前記酸形態のアニオン系界面活性剤を均一に繊維表面に分散させることができる。   In particular, when the acid form anionic surfactant is melted and kneaded with the olefin polymer, the effect of reducing skin irritation is preferred. Further, when the nonionic surfactant is used in combination, melt kneading is improved by melt kneading together with the acid form anionic surfactant, and the nonionic surfactant and the acid form of the acid form are improved. An anionic surfactant can be uniformly dispersed on the fiber surface.

本発明の繊維は、通常、繊度が0.5〜5デニールの範囲にある。本発明の繊維は短繊維であってもよいが、長繊維であることが、得られる不織布からの繊維の脱落等がないので好ましい。   The fibers of the present invention usually have a fineness in the range of 0.5 to 5 denier. Although the fiber of the present invention may be a short fiber, it is preferable that the fiber is a long fiber because the fiber does not fall off from the resulting nonwoven fabric.

本発明の繊維の断面形状は丸型の他にV字型、十字型、T字型などの異型断面であっても良い。   The cross-sectional shape of the fiber of the present invention may be an irregular cross-section such as a V shape, a cross shape, or a T shape in addition to a round shape.

本発明の繊維は、サイド・バイ・サイド型の少なくとも2成分以上のオレフィン系重合体組成物からなる捲縮繊維であっても良い。好ましくは、オレフィン系重合体として、プロピレンの単独重合体とプロピレン・エチレンランダム共重合体からなるサイド・バイ・サイド型の捲縮繊維を挙げることができる。   The fiber of the present invention may be a crimped fiber made of an olefin polymer composition having at least two components of side-by-side type. Preferably, examples of the olefin polymer include side-by-side crimped fibers made of a propylene homopolymer and a propylene / ethylene random copolymer.

また、本発明の繊維は、同芯型あるいは偏芯型の繊維であってもよく、その場合は、芯部、鞘部の両方、あるいはいずれか一方に、前記酸形態のアニオン系界面活性剤及び好ましくは前記ノニオン系界面活性剤を添加しても良い。   In addition, the fiber of the present invention may be a concentric or eccentric fiber, and in that case, the acid form anionic surfactant may be provided in both or either of the core part and the sheath part. And preferably, the nonionic surfactant may be added.

さらに、本発明の繊維は、他の繊維との混繊不織布としてもよい。例えば、本発明の繊維は、かかる捲縮繊維とその他の非捲縮繊維との混繊不織布としても良い。   Furthermore, the fiber of the present invention may be a mixed nonwoven fabric with other fibers. For example, the fibers of the present invention may be a mixed nonwoven fabric of such crimped fibers and other non-crimped fibers.

本発明の不織布は、通常、目付が10〜30g/m2、好ましくは15〜25g/m2の範囲にある。The nonwoven fabric of the present invention usually has a basis weight of 10 to 30 g / m 2 , preferably 15 to 25 g / m 2 .

本発明の不織布は、用途により、種々公知の交絡方法、例えば、ニードルパンチ、ウォータージェット、超音波等の手段を用いる方法、あるいはエンボスロールを用いる熱エンボス加工またはホットエアースルーを用いることにより一部熱融着する方法により交絡しておいてもよい。かかる交絡方法は単独でも複数の交絡方法を組み合わせて用いてもよい。   The nonwoven fabric of the present invention is partially used by various known entanglement methods, for example, a method using means such as needle punching, water jet, and ultrasonic waves, or hot embossing using an embossing roll or hot air through. It may be entangled by a method of heat fusion. Such entanglement methods may be used alone or in combination with a plurality of entanglement methods.

熱エンボス加工により熱融着する場合は、通常、エンボス面積率が3〜30%、好ましくは5〜20%の範囲にある。刻印形状は、円、楕円、長円、正方、菱、長方、四角、キルト、格子、亀甲やそれら形状を基本とする連続した形が例示される。   When heat-sealing by hot embossing, the embossed area ratio is usually in the range of 3 to 30%, preferably 5 to 20%. Examples of the stamped shape include a circle, an ellipse, an ellipse, a square, a rhombus, a rectangle, a square, a quilt, a lattice, a turtle shell, and a continuous shape based on these shapes.

本発明の不織布は、種々用途により、単独でも他の層と積層して用いてもよい。   The nonwoven fabric of the present invention may be used alone or laminated with other layers depending on various applications.

本発明の不織布と積層される他の層は、具体的には、例えば、編布、織布、不織布、フィルム、紙製品等を挙げることができる。本発明の不織布と他の層を積層する(貼り合せる)場合は、熱エンボス加工、超音波融着等の熱融着法、ニードルパンチ、ウォータージェット等の機械的交絡法、ホットメルト接着剤、ウレタン系接着剤等の接着剤による方法、押出しラミネート等をはじめ、種々公知の方法を採り得る。本発明の不織布は、ホットメルト接着剤や押出しラミネート等、高温物質と接触する工程を経た後も、かぶれ低減効果が持続するので、製品の品質管理上、利便性が高い。   Specifically, the other layer laminated | stacked with the nonwoven fabric of this invention can mention a knitted fabric, a woven fabric, a nonwoven fabric, a film, a paper product etc., for example. When laminating (bonding) the nonwoven fabric of the present invention and other layers, thermal embossing, thermal fusion methods such as ultrasonic fusion, mechanical entanglement methods such as needle punch and water jet, hot melt adhesive, Various known methods such as a method using an adhesive such as a urethane-based adhesive, extrusion lamination, and the like can be adopted. The nonwoven fabric of the present invention is highly convenient in terms of product quality control because the rash reduction effect continues even after a process of contacting with a high-temperature substance such as a hot melt adhesive or an extrusion laminate.

本発明の不織布と積層される不織布としては、他のスパンボンド不織布、メルトブロー不織布、湿式不織布、乾式不織布、乾式パルプ不織布、フラッシュ紡糸不織布、開繊不織布等、種々公知の不織布を挙げることができる。   Examples of the nonwoven fabric laminated with the nonwoven fabric of the present invention include other known nonwoven fabrics such as other spunbond nonwoven fabrics, melt blown nonwoven fabrics, wet nonwoven fabrics, dry nonwoven fabrics, dry pulp nonwoven fabrics, flash spun nonwoven fabrics, and spread nonwoven fabrics.

かかる不織布を構成する材料としては、種々公知の熱可塑性樹脂、例えば、エチレン、プロピレン、1−ブテン、1−ヘキセン、4−メチル−1−ペンテン及び1−オクテン等のα−オレフィンの単独若しくは共重合体である高圧法低密度ポリエチレン、線状低密度ポリエチレン(所謂LLDPE)、高密度ポリエチレン、ポリプロピレン、ポリプロピレンランダム共重合体、ポリ1−ブテン、ポリ4−メチル−1−ペンテン、エチレン・プロピレンランダム共重合体、エチレン・1−ブテンランダム共重合体、プロピレン・1−ブテンランダム共重合体等のポリオレフィン、ポリエステル(ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリエチレンナフタレート等)、ポリアミド(ナイロン−6、ナイロン−66、ポリメタキシレンアジパミド等)、ポリ塩化ビニル、ポリイミド、エチレン・酢酸ビニル共重合体、ポリアクリロニトリル、ポリカーボネート、ポリスチレン、アイオノマー、熱可塑性ポリウレタンあるいはこれらの混合物等を例示することができる。これらのうちでは、高圧法低密度ポリエチレン、線状低密度ポリエチレン(所謂LLDPE)、高密度ポリエチレン、ポリプロピレン、ポリプロピレンランダム共重合体、ポリエチレンテレフタレート、ポリアミド等が好ましい。   Examples of the material constituting such a nonwoven fabric include various known thermoplastic resins such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, and 1-octene and other α-olefins. High pressure low density polyethylene, linear low density polyethylene (so-called LLDPE), high density polyethylene, polypropylene, polypropylene random copolymer, poly 1-butene, poly 4-methyl-1-pentene, ethylene / propylene random Polyolefin such as copolymer, ethylene / 1-butene random copolymer, propylene / 1-butene random copolymer, polyester (polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, etc.), polyamide (nylon-6, nylon- 66, polymer Xylene adipamide, etc.), polyvinyl chloride, polyimide, ethylene-vinyl acetate copolymer, polyacrylonitrile, polycarbonate can be exemplified polystyrene, ionomers, thermoplastic polyurethane, or mixtures thereof. Among these, high pressure method low density polyethylene, linear low density polyethylene (so-called LLDPE), high density polyethylene, polypropylene, polypropylene random copolymer, polyethylene terephthalate, polyamide and the like are preferable.

本発明の不織布と積層される他のスパンボンド不織布として、捲縮繊維より成る不織布を用いると、得られる積層体は、柔軟性、嵩高性、及び触感に優れる。また、熱可塑性樹脂及び熱可塑性エラストマーそれぞれの長繊維の混合繊維より成る不織布を延伸加工したものを用いると、得られる積層体は、前記特徴に加えて、伸縮性に優れる。   When a nonwoven fabric made of crimped fibers is used as another spunbond nonwoven fabric laminated with the nonwoven fabric of the present invention, the resulting laminate is excellent in flexibility, bulkiness, and touch. Moreover, when the thing which extended | stretched the nonwoven fabric which consists of a mixed fiber of each thermoplastic resin and a thermoplastic elastomer is used, in addition to the said characteristic, the laminated body obtained is excellent in a stretching property.

本発明の不織布を吸収性物品、例えば、使い捨ておむつのトップシート、セカンドシートあるいは吸収体を包むシート(コアラップ)に用いる場合は、繊度を0.5〜3デニール、目付を7〜50g/m2の範囲とすることが好ましい。When the nonwoven fabric of the present invention is used for an absorbent article, for example, a disposable diaper top sheet, a second sheet, or a sheet (core wrap) that wraps an absorbent body, the fineness is 0.5 to 3 denier and the basis weight is 7 to 50 g / m 2. It is preferable to set it as the range.

また、本発明の不織布を吸収性物品の吸収体を包むシート(コアラップ)に用いる場合は、前記メルトブロー不織布と積層して用いてもよい。   Moreover, when using the nonwoven fabric of this invention for the sheet | seat (core wrap) which wraps the absorber of an absorbent article, you may laminate | stack with the said melt blown nonwoven fabric.

本発明の不織布と積層されるフィルムとしては、本発明の不織布の特徴であるかぶれ低減効果がより生かされるよう、通気性(透湿性)フィルムが好ましい。かかる通気性フィルムとしては、種々公知の通気性フィルム、例えば、透湿性を有するポリウレタン系エラストマー、ポリエステル系エラストマー、ポリアミド系エラストマー等の熱可塑性エラストマーからなるフィルム、無機あるいは有機微粒子を含む熱可塑性樹脂からなるフィルムを延伸して多孔化してなる多孔フィルム等を挙げることができる。多孔フィルムに用いる熱可塑性樹脂としては、高圧法低密度ポリエチレン、線状低密度ポリエチレン(所謂LLDPE)、高密度ポリエチレン、ポリプロピレン、ポリプロピレンランダム共重合体あるいはそれらの組成物等のポリオレフィンが好ましい。   The film laminated with the nonwoven fabric of the present invention is preferably a breathable (moisture permeable) film so that the rash reduction effect that is a feature of the nonwoven fabric of the present invention can be utilized. Examples of such a breathable film include various known breathable films, for example, films made of thermoplastic elastomers such as moisture-permeable polyurethane elastomers, polyester elastomers, polyamide elastomers, and thermoplastic resins containing inorganic or organic fine particles. Examples thereof include a porous film formed by stretching a film to be porous. The thermoplastic resin used for the porous film is preferably a polyolefin such as high-pressure method low-density polyethylene, linear low-density polyethylene (so-called LLDPE), high-density polyethylene, polypropylene, polypropylene random copolymer, or a composition thereof.

本発明の不織布は、本発明の目的を損なわない範囲で、ギア加工、印刷、塗布、ラミネート、熱処理、賦型加工などの二次加工を施して用いてもよい。   The non-woven fabric of the present invention may be used after being subjected to secondary processing such as gear processing, printing, coating, laminating, heat treatment, and shaping, as long as the object of the present invention is not impaired.

<不織布の製造方法>
不織布の原料として短繊維を用いる場合は、種々公知の製造方法、例えば、湿式法あるいは乾式法(カード)により製造し得る。
<Nonwoven Fabric Manufacturing Method>
When short fibers are used as the raw material for the nonwoven fabric, they can be produced by various known production methods, for example, a wet method or a dry method (card).

<長繊維不織布の製造方法>
本発明の長繊維不織布は、種々公知の不織布の製造方法により製造し得るが、スパンボンド法により製造する方法が、生産性に優れる点で好ましい。
<Method for producing long-fiber nonwoven fabric>
The long-fiber nonwoven fabric of the present invention can be produced by various known methods for producing nonwoven fabrics, but the method produced by the spunbond method is preferred in terms of excellent productivity.

本発明の長繊維不織布をスパンボンド法により製造する場合は、オレフィン系重合体組成物の単繊維からなるスパンボンド不織布を製造する場合は1つの押出機で180〜250℃、好ましくは190〜230℃で溶融し、紡糸ノズルを有する180〜250℃、好ましくは190〜230℃に設定した紡糸口金から0.4〜1.5 g/分、好ましくは0.5〜0.8g/分の単孔吐出量で吐出させて、繊維を紡出し、紡出した繊維を10〜40℃、好ましくは20〜40℃の冷却用エアにより冷却するとともに、2000〜7000m/分、好ましくは3000〜6000m/分の高速エアにより繊維を牽引細化して所定の繊度とし、捕集ベルト上に捕集して所定の厚さ(目付)に堆積させた後、ニードルパンチ、ウォータージェット、超音波等の手段を用いる方法、あるいはエンボスロールを用いる熱エンボス加工またはホットエアースルーを用いることにより一部熱融着する方法等の交絡方法で交絡することにより製造し得る。   When producing the long-fiber nonwoven fabric of the present invention by the spunbond method, when producing a spunbond nonwoven fabric comprising single fibers of the olefin polymer composition, 180 to 250 ° C, preferably 190 to 230, with one extruder. From 0.4 to 1.5 g / min, preferably 0.5 to 0.8 g / min from a spinneret melted at ℃ and having a spinning nozzle set at 180 to 250 ° C., preferably 190 to 230 ° C. The fiber is spun by discharging with a hole discharge amount, and the spun fiber is cooled by cooling air at 10 to 40 ° C., preferably 20 to 40 ° C., and 2000 to 7000 m / min, preferably 3000 to 6000 m / min. After pulling the fiber with high-speed air for a minute to a predetermined fineness, collecting it on a collection belt and depositing it on a predetermined thickness (weight), needle punch, water jet, supersonic sound The method using means of equal or may be prepared by entangling by entangling method and a method of thermal fusion portion by using a heat embossing or hot air-through using an embossing roll.

<吸収性物品>
本発明の吸収性物品は、前記不織布、好ましくは長繊維不織布をトップシート及び/又はセカンドシート、あるいは吸収体を包むシート(コアラップ)に用いてなる吸収性物品である。本発明の吸収性物品は、使い捨ておむつ、パンツあるいは生理用品、尿取りパッド、ペット用シートなどを含む。
<Absorbent article>
The absorbent article of the present invention is an absorbent article formed by using the nonwoven fabric, preferably a long fiber nonwoven fabric, as a top sheet and / or a second sheet, or a sheet (core wrap) that wraps an absorbent body. The absorbent article of the present invention includes disposable diapers, pants or sanitary products, urine collection pads, pet sheets and the like.

とくに、使い捨ておむつのトップシート、セカンドシートあるいは吸収体を包むシート(コアラップ)に用いる場合、オレフィン系重合体組成物の繊維からなる不織布を用いる場合は、オレフィン系重合体100重量部に対して、酸形態のアニオン系界面活性剤を0.5〜30重量部、或いは酸形態のアニオン系界面活性剤を0.5〜30重量部、及びノニオン系界面活性剤を0.5〜30重量部含むことが好ましい。   In particular, when using a disposable diaper top sheet, a second sheet or a sheet (core wrap) that wraps the absorbent body, when using a nonwoven fabric made of fibers of an olefin polymer composition, 100 parts by weight of the olefin polymer, 0.5-30 parts by weight of an anionic surfactant in acid form, or 0.5-30 parts by weight of an anionic surfactant in acid form, and 0.5-30 parts by weight of a nonionic surfactant It is preferable.

以下、実施例に基づいて本発明をさらに具体的に説明するが、本発明はこれらの実施例に限定されるものではない。   EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example, this invention is not limited to these Examples.

なお、実施例及び比較例におけるかぶれ抑制効果の程度は、以下の方法により評価した。   In addition, the following methods evaluated the degree of the rash suppression effect in an Example and a comparative example.

〔かぶれ評価方法〕
以下の手順にてかぶれの程度を評価した。
[Rash evaluation method]
The degree of rash was evaluated by the following procedure.

健康な3歳児(男)から採取した便を蒸留水にて1%に希釈し、(株)コクサン社製冷却高速遠心分離機H−201FRを用い、3000rpm−15分間遠心分離した上澄み液を採取して評価液とした。この評価液に、以下の実施例、及び比較例で製造した不織布サンプルを1分、及び30分間浸した後、ISO10993−10(炎症および遅効性過敏症のための試験)に基づき調整したうさぎ3匹の皮膚に貼付し、48時間後の皮膚の状態を観察した。   Dilute feces collected from a healthy 3-year-old child (male) to 1% with distilled water, and collect the supernatant obtained by centrifugation at 3000 rpm for 15 minutes using a cooling high-speed centrifuge H-201FR manufactured by Kokusan Co., Ltd. And used as an evaluation solution. After immersing the nonwoven fabric samples produced in the following Examples and Comparative Examples for 1 minute and 30 minutes in this evaluation solution, the rabbit 3 was prepared based on ISO 10993-10 (test for inflammation and delayed hypersensitivity). It was affixed to the skin of a mouse and the state of the skin 48 hours later was observed.

〔評価基準〕
1点:3匹とも皮膚の状態に殆ど変化がなかった。
〔Evaluation criteria〕
1 point: All three animals had almost no change in skin condition.

2点:1〜2匹に、僅かに浮腫、斑点が現れた。       2 points: Slight edema and spots appeared in 1 to 2 animals.

3点:3匹とも、僅かに浮腫、斑点が現れた。       3 points: Slight edema and spots appeared in all 3 animals.

4点:1〜2匹に浮腫、斑点が現れた。       4 points: Edema and spots appeared in 1 to 2 animals.

5点:3匹とも浮腫、斑点が現れた。       5 points: Edema and spots appeared in all 3 animals.

6点:3匹とも浮腫、斑点が顕著に現れた。       6 points: All three animals showed marked edema and spots.

〔押出成型性〕
1点:押出機スクリューへの食込み状態良好。
[Extrudability]
1 point: Good biting into the extruder screw.

2点:押出機スクリューへの食込み状態に難あり。ノズル圧力変動あり。       2 points: Difficult to bite into the extruder screw. There is nozzle pressure fluctuation.

[実施例1]
オレフィン系重合体100重量部に対して酸形態のアニオン系界面活性剤、あるいはノニオン系界面活性剤が表1記載の量含む組成物を以下のようにして調整した。酸形態のアニオン系界面活性剤としてステアリン酸(花王社製、商品名ルナックS−90V)10重量部、及びノニオン系界面活性剤としてステアリルアルコールのエチレンオキサイド付加物(BASF社(旧Ciba社)製、Irgasurf HL560)10重量部を、融点(Tm):142℃、MFR:60g/10分のプロピレン・エチレンランダム共重合体(PP−1):79.95重量部、酸化防止剤(BASF社(旧Ciba社)製、商品名Irgafos168)を0.05重量部と共に230℃で溶融混練して押出し、ペレット状のマスターバッチ(MB―1)を用意した。
[Example 1]
A composition containing an anionic surfactant in acid form or a nonionic surfactant in an amount shown in Table 1 with respect to 100 parts by weight of the olefin polymer was prepared as follows. 10 parts by weight of stearic acid (trade name Lunac S-90V, manufactured by Kao Corporation) as an anionic surfactant in acid form, and ethylene oxide adduct of stearyl alcohol (BASF (former Ciba)) as a nonionic surfactant , Irgasurf HL560), melting point (Tm): 142 ° C., MFR: 60 g / 10 min propylene / ethylene random copolymer (PP-1): 79.95 parts by weight, antioxidant (BASF ( A product name Irgafos 168) manufactured by the former Ciba company) was melt-kneaded at 230 ° C. together with 0.05 parts by weight and extruded to prepare a pellet-like masterbatch (MB-1).

次いで、PP−1を60重量部に対して、前記MB−1を40重量部加えて混合し、プロピレン系重合体組成物(組成物−1)を得た。   Subsequently, 40 parts by weight of the MB-1 was added to 60 parts by weight of PP-1 and mixed to obtain a propylene polymer composition (Composition-1).

押出性能を評価するために、組成物‐1を、単軸押出機(スクリュー径30mm、L/D=30)に投入し、押出量4.4kg/hr、樹脂温度200℃にて加熱溶融させたところ、押出機スクリューへの組成物−1の食込み状態は界面活性剤を加えない時と同様で良好であった。   In order to evaluate the extrusion performance, the composition-1 was put into a single screw extruder (screw diameter 30 mm, L / D = 30) and melted by heating at an extrusion rate of 4.4 kg / hr and a resin temperature of 200 ° C. As a result, the biting state of Composition-1 into the extruder screw was as good as when no surfactant was added.

次いで、組成物‐1を用いて、スパンボンド法により溶融紡糸し、長繊維不織布を得た。紡糸に続いて刻印形状が菱形、エンボス面積率が18%、エンボス面積(刻印一つ当たりの面積)が0.41mm2のエンボスロールを用いて、エンボスロールおよび平滑ロールの温度を125℃、線圧力を60N/mmとして熱エンボス加工し、目付けが20g/m2の長繊維不織布を得た。得られた長繊維不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表1に示す。Subsequently, the composition-1 was melt-spun by a spunbond method to obtain a long fiber nonwoven fabric. Following spinning, the embossing roll has a rhombus shape, an embossing area ratio of 18%, and an embossing area (area per imprinting) of 0.41 mm 2. Heat embossing was performed at a pressure of 60 N / mm to obtain a long fiber nonwoven fabric having a basis weight of 20 g / m 2 . Using the obtained long-fiber nonwoven fabric, the degree of rash was evaluated by the above-described rash evaluation method. The results are shown in Table 1.

[実施例2〜6]
酸形態のアニオン系界面活性剤、及びノニオン系界面活性剤として、以下の化合物を用い、且つ、添加量を表1に示す通りに変更する以外は実施例1と同様に行い、長繊維不織布を得た。得られた長繊維不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表1に示す。
[Examples 2 to 6]
As the anionic surfactant in the acid form and the nonionic surfactant, the following compounds were used, and the same procedure was performed as in Example 1 except that the addition amount was changed as shown in Table 1. Obtained. Using the obtained long-fiber nonwoven fabric, the degree of rash was evaluated by the above-described rash evaluation method. The results are shown in Table 1.

ミリスチン酸(C14):花王社製 商品名 ルナックMY−98
オレス−4リン酸(C18):東邦化学工業社製 商品名 フォスファノールRB−410
[実施例7]
オレフィン系重合体100重量部に対して酸形態のアニオン系界面活性剤、あるいはノニオン系界面活性剤が表1記載の量含む組成物を以下のようにして調整した。酸形態のアニオン系界面活性剤としてドデシルリン酸(竹本油脂社製)5重量部、及びノニオン系界面活性剤としてポリ(オキシエチレン)1,6-ヘキサンジオール・ジラウレート(竹本油脂社製)14重量部、ポリ(オキシエチレン)ソルビタン三オレイン酸エステル(竹本油脂社製)1重量部を、融点(Tm):142℃、MFR:60g/10分のプロピレン・エチレンランダム共重合体(PP−1):79.95重量部、酸化防止剤(BASF社(旧Ciba社)製、商品名Irganox1010)を0.05重量部と共に180℃で溶融混練して押出し、ペレット状のマスターバッチ(MB―2)を用意した。
Myristic acid (C14): trade name, Lunac MY-98, manufactured by Kao Corporation
Ores-4-phosphate (C18): Toho Chemical Industries, Ltd. Product name Phosphanol RB-410
[Example 7]
A composition containing an anionic surfactant in acid form or a nonionic surfactant in an amount shown in Table 1 with respect to 100 parts by weight of the olefin polymer was prepared as follows. 5 parts by weight of dodecyl phosphate (manufactured by Takemoto Yushi Co., Ltd.) as an anionic surfactant in acid form, and 14 parts by weight of poly (oxyethylene) 1,6-hexanediol dilaurate (manufactured by Takemoto Yushi Co., Ltd.) as a nonionic surfactant 1 part by weight of poly (oxyethylene) sorbitan trioleate (manufactured by Takemoto Yushi Co., Ltd.), propylene / ethylene random copolymer (PP-1) having a melting point (Tm): 142 ° C. and MFR: 60 g / 10 min: 79.95 parts by weight, antioxidant (manufactured by BASF (former Ciba), trade name Irganox 1010) was melt kneaded at 180 ° C. together with 0.05 parts by weight, and extruded into a master batch (MB-2). Prepared.

次いで、PP−1を80重量部に対して、前記MB−2を20重量部加えて混合し、プロピレン系重合体組成物(組成物−2)を得た。   Next, 20 parts by weight of MB-2 was added to 80 parts by weight of PP-1 and mixed to obtain a propylene polymer composition (Composition-2).

押出性能を評価するために、組成物‐2を、単軸押出機(スクリュー径30mm、L/D=30)に投入し、押出量4.4kg/hr、樹脂温度200℃にて加熱溶融させたところ、押出機スクリューへの組成物−2の食込み状態は界面活性剤を加えない時と同様で良好であった。   In order to evaluate the extrusion performance, composition-2 was put into a single screw extruder (screw diameter 30 mm, L / D = 30), and melted by heating at an extrusion rate of 4.4 kg / hr and a resin temperature of 200 ° C. As a result, the biting state of Composition-2 into the extruder screw was as good as when no surfactant was added.

次いで、組成物‐2を用いて、スパンボンド法により溶融紡糸し、長繊維不織布を得た。紡糸に続いて刻印形状が菱形、エンボス面積率が18%、エンボス面積(刻印一つ当たりの面積)が0.41mm2のエンボスロールを用いて、エンボスロールおよび平滑ロールの温度を125℃、線圧力を60N/mmとして熱エンボス加工し、目付けが20g/m2の長繊維不織布を得た。得られた長繊維不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表1に示す。Subsequently, the composition-2 was melt-spun by a spunbond method to obtain a long fiber nonwoven fabric. Following spinning, the embossing roll has a rhombus shape, an embossing area ratio of 18%, and an embossing area (area per imprinting) of 0.41 mm 2. Heat embossing was performed at a pressure of 60 N / mm to obtain a long fiber nonwoven fabric having a basis weight of 20 g / m 2 . Using the obtained long-fiber nonwoven fabric, the degree of rash was evaluated by the above-described rash evaluation method. The results are shown in Table 1.

[実施例8、9]
実施例7で用いたノニオン系界面活性剤を用い、酸形態のアニオン系界面活性剤として以下の化合物を用い、且つ、添加量を表1に示す通りに変更する以外は実施例7と同様に行い、長繊維不織布を得た。得られた長繊維不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表1に示す。
[Examples 8 and 9]
Similar to Example 7 except that the nonionic surfactant used in Example 7 was used, the following compound was used as the anionic surfactant in the acid form, and the addition amount was changed as shown in Table 1. The long fiber nonwoven fabric was obtained. Using the obtained long-fiber nonwoven fabric, the degree of rash was evaluated by the above-described rash evaluation method. The results are shown in Table 1.

アニオン系界面活性剤
オクチルリン酸(C8):竹本油脂社製
オクタデカン-1-イル= 二水素=ホスファート(C18):竹本油脂社製
リン酸水素ジオクタデシル(C18):竹本油脂社製
Anionic surfactant Octyl phosphoric acid (C8): Takemoto Yushi Co., Ltd. Octadecan-1-yl dihydrogen = phosphate (C18): Takemoto Yushi Co., Ltd. Hydrogen dioctadecyl phosphate (C18): Takemoto Yushi Co., Ltd.

Figure 0005819410
Figure 0005819410

[比較例1]
実施例1で用いたノニオン系界面活性剤のみを添加し、酸形態のアニオン系界面活性剤を添加しない点以外は実施例1と同様に行い、長繊維不織布を得た。得られた長繊維不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表2に示す。
[Comparative Example 1]
A long fiber nonwoven fabric was obtained in the same manner as in Example 1 except that only the nonionic surfactant used in Example 1 was added and no anionic surfactant in acid form was added. Using the obtained long-fiber nonwoven fabric, the degree of rash was evaluated by the above-described rash evaluation method. The results are shown in Table 2.

[比較例2〜6]
PP−1を用いてスパンボンド法により溶融紡糸し、長繊維不織布を得た。紡糸に続いて刻印形状が菱形、エンボス面積率が18%、エンボス面積(刻印一つ当たりの面積)が0.41mm2のエンボスロールを用いて、エンボスロールおよび平滑ロールの温度を125℃、線圧力を60N/mmとして熱エンボス加工し、目付けが20g/m2の長繊維不織布(NW−1)を得た。一方、表2で示す比較例2〜6として、以下の化合物を、各々が溶解可能な濃度に調整したイソプロピルアルコール水溶液に溶解し、塗布液を得、これをNW−1に塗布し、その後乾燥させる。塗布、乾燥を繰り返し、乾燥後の重量が表2で示す所定の添加量になるよう調整した。得られた不織布を用いて、前記記載のかぶれ評価方法によりかぶれの程度を評価した。結果を表2に示す。
[Comparative Examples 2 to 6]
PP-1 was melt-spun by a spunbond method to obtain a long fiber nonwoven fabric. Following spinning, the embossing roll has a rhombus shape, an embossing area ratio of 18%, and an embossing area (area per imprinting) of 0.41 mm 2. Thermal embossing was performed at a pressure of 60 N / mm to obtain a long fiber nonwoven fabric (NW-1) having a basis weight of 20 g / m 2 . On the other hand, as Comparative Examples 2 to 6 shown in Table 2, the following compounds were dissolved in an isopropyl alcohol aqueous solution adjusted to a concentration at which each can be dissolved to obtain a coating solution, which was applied to NW-1, and then dried. Let Coating and drying were repeated, and the weight after drying was adjusted to a predetermined addition amount shown in Table 2. Using the obtained nonwoven fabric, the degree of rash was evaluated by the rash evaluation method described above. The results are shown in Table 2.

アニオン系界面活性剤
クエン酸(C6):和光純薬工業社製 試薬
オクチル酸(C8):協和発酵ケミカル社製 試薬
ステアリルアルコール(C18):花王社製 商品名 カルコール8098
ドデシルリン酸(C12):竹本油脂社製
ノニオン系界面活性剤
ポリ(オキシエチレン)1,6-ヘキサンジオール・ジラウレート:竹本油脂社製
ポリ(オキシエチレン)ソルビタン三オレイン酸エステル(竹本油脂社製)
Anionic surfactant Citric acid (C6): Reagent manufactured by Wako Pure Chemical Industries, Ltd. Octyl acid (C8): Reagent manufactured by Kyowa Hakko Chemical Co., Ltd. Stearyl alcohol (C18): manufactured by Kao Corporation Product name Calcoal 8098
Dodecyl phosphoric acid (C12): Nonionic surfactant poly (oxyethylene) 1,6-hexanediol dilaurate manufactured by Takemoto Yushi Co., Ltd. Poly (oxyethylene) sorbitan trioleate (manufactured by Takemoto Yushi Co., Ltd.)

Figure 0005819410
Figure 0005819410

本発明の繊維及び当該繊維を含む不織布は、紙おむつ、生理用品などの衛生材料のトップシート、またはセカンドシートとして好適に使用することができる。   The fiber of this invention and the nonwoven fabric containing the said fiber can be used conveniently as a top sheet of sanitary materials, such as a paper diaper and sanitary goods, or a second sheet.

Claims (6)

融点(Tm)が125〜155℃の範囲にあるプロピレンと、α−オレフィンからなるプロピレン・α−オレフィンランダム共重合体100重量部に対して、炭素数が9以上の脂肪酸である酸形態のアニオン系界面活性剤を0.1〜30重量部含むオレフィン系重合体組成物からなる繊維であって、前記炭素数が9以上の脂肪酸である酸形態のアニオン系界面活性剤が、繊維に溶融混錬されてなる繊維。 An anion in the form of an acid which is a fatty acid having 9 or more carbon atoms with respect to 100 parts by weight of a propylene / α-olefin random copolymer composed of propylene having a melting point (Tm) of 125 to 155 ° C. and an α-olefin. A fiber comprising an olefin polymer composition containing 0.1 to 30 parts by weight of a surfactant, wherein the anionic surfactant in the acid form, which is a fatty acid having 9 or more carbon atoms, is melt mixed into the fiber. Refined fiber. オレフィン系重合体組成物がノニオン系界面活性剤を0.1〜30重量部含む請求項1に記載の繊維。   The fiber according to claim 1, wherein the olefin polymer composition contains 0.1 to 30 parts by weight of a nonionic surfactant. 繊維が長繊維である請求項1または2に記載の繊維。 The fiber according to claim 1 or 2 , wherein the fiber is a long fiber. 請求項に記載の繊維からなる不織布。 A nonwoven fabric comprising the fiber according to claim 3 . 請求項に記載の不織布を、トップシート及び/又はセカンドシートに用いてなる吸収性物品。 The absorbent article which uses the nonwoven fabric of Claim 4 for a top sheet and / or a second sheet. 請求項に記載の不織布を、吸収体を包むシートに用いてなる吸収性物品。 The absorbent article which uses the nonwoven fabric of Claim 4 for the sheet | seat which wraps an absorber.
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Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6092578B2 (en) * 2012-11-07 2017-03-08 旭化成株式会社 Weakly acid permeable nonwoven fabric
CN104562257B (en) * 2015-01-06 2016-10-19 陈康振 A kind of non-woven fabrics or the special additive of fiber and preparation method thereof and non-woven fabrics
JP6678643B2 (en) * 2015-03-04 2020-04-08 ダイワボウホールディングス株式会社 Rayon fiber for air-laid non-woven fabric and its manufacturing method, air-laid non-woven fabric and its manufacturing method, and hydrolyzed paper
MY186916A (en) * 2016-03-09 2021-08-26 Fibertex Personal Care As High barrier nonwoven fabric
JP6687484B2 (en) * 2016-08-30 2020-04-22 ユニ・チャーム株式会社 Fiber treatment agent for absorbent articles, fibers, non-woven fabrics and absorbent articles
JP6980954B2 (en) * 2016-11-22 2021-12-15 大和紡績株式会社 Masterbatch resin composition, its manufacturing method, and a molded product processed from this
JP2018117866A (en) * 2017-01-25 2018-08-02 王子ホールディングス株式会社 Absorbent article
JP6870480B2 (en) * 2017-05-30 2021-05-12 東レ株式会社 Polyethylene spunbonded non-woven fabric
KR102006816B1 (en) * 2018-01-26 2019-10-01 도레이첨단소재 주식회사 Nonwoven fabric having an excellent hygroscopicity
CN111868313B (en) * 2018-03-29 2022-12-02 陶氏环球技术有限责任公司 Bicomponent fibers and polymer compositions thereof
JP7048150B2 (en) * 2018-03-29 2022-04-05 三井化学株式会社 Non-woven fabric
CN111485325A (en) * 2020-04-16 2020-08-04 青岛科技大学 High-temperature-resistant antibacterial nanofiber non-woven fabric and preparation method and application thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0253950A (en) * 1988-08-12 1990-02-22 Kuraray Co Ltd Production of hydrophilic non woven fabric
JPH11323715A (en) * 1998-05-14 1999-11-26 Mitsui Chem Inc Top sheet material for absorptive article
JP2002161428A (en) * 2000-11-29 2002-06-04 Nippon Supplement Kk METHOD FOR PRODUCING gamma-LINOLENIC ACID-CONTAINING FIBER
JP2003500556A (en) * 1999-05-21 2003-01-07 スリーエム イノベイティブ プロパティズ カンパニー Hydrophilic polypropylene fiber with antibacterial activity
JP2008535955A (en) * 2005-03-14 2008-09-04 ロディア ルシェルシュ エ テクノロジー Composition comprising a thermoplastic polymer and a hydrophilizing agent
JP2010150674A (en) * 2008-12-24 2010-07-08 Mitsui Chemicals Inc Fiber and nonwoven fabric

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE599410A (en) * 1960-01-23
US3231530A (en) * 1962-07-06 1966-01-25 Monsanto Co Dyeable polypropylene-stearic acid compositions
US3973068A (en) * 1975-10-28 1976-08-03 Kimberly-Clark Corporation Soft, nonwoven web having high intensity and low intensity bonds and a lubricant on the surfaces of the synthetic filaments comprising said
US4323534A (en) * 1979-12-17 1982-04-06 The Procter & Gamble Company Extrusion process for thermoplastic resin composition for fabric fibers with exceptional strength and good elasticity
US5434182A (en) * 1987-12-31 1995-07-18 Isaacs; Charles E. Antibacterial fatty acid compositions
US4996238A (en) * 1988-09-16 1991-02-26 Neutrogena Corporation Method of treating diaper rash
JP2682130B2 (en) * 1989-04-25 1997-11-26 三井石油化学工業株式会社 Flexible long-fiber non-woven fabric
US5430119A (en) * 1991-06-11 1995-07-04 Mitsui Petrochemical Industries, Ltd. Stretched molded article of ultra-high-molecular weight polypropylene and process for the preparation of the same
US5814404A (en) * 1994-06-03 1998-09-29 Minnesota Mining And Manufacturing Company Degradable multilayer melt blown microfibers
DE69633420T2 (en) * 1995-03-31 2005-09-29 Basell North America Inc. High energy radiation resistant polyolefin compositions and articles made therefrom
US5804512A (en) * 1995-06-07 1998-09-08 Bba Nonwovens Simpsonville, Inc. Nonwoven laminate fabrics and processes of making same
JP3475596B2 (en) * 1995-08-01 2003-12-08 チッソ株式会社 Durable hydrophilic fibers, cloths and moldings
ZA992005B (en) 1998-03-12 1999-09-13 Procter & Gamble Proton donating actives in absorbent articles.
US6696373B2 (en) * 1999-01-08 2004-02-24 Bba Nonwovens Simpsonville, Inc. Durable hydrophilic nonwoven webs and articles formed therefrom
US6459014B1 (en) 1999-11-15 2002-10-01 Paragon Trade Brands, Inc. Absorbent article which maintains prolonged natural skin pH
JP4009196B2 (en) * 2001-01-29 2007-11-14 三井化学株式会社 Crimped fiber nonwoven fabric and laminate thereof
US20040158214A1 (en) * 2003-02-10 2004-08-12 The Procter & Gamble Company Disposable absorbent article comprising a durable hydrophilic topsheet
US7063917B2 (en) * 2001-02-21 2006-06-20 Ahlstrom Mount Holly Springs, Llc Laminated battery separator material
JPWO2002083121A1 (en) * 2001-04-12 2005-01-27 勝守 福本 Skin environment improving composition and clothes thereof
US7585563B2 (en) * 2001-05-01 2009-09-08 Ocv Intellectual Capital, Llc Fiber size, sized reinforcements, and articles reinforced with such reinforcements
JP4206211B2 (en) * 2001-10-31 2009-01-07 日本ポリプロ株式会社 Non-woven fabric for battery separator
US7192896B2 (en) * 2001-11-15 2007-03-20 3M Innovative Properties Company Disposable cleaning product
DE10206111A1 (en) * 2002-02-13 2003-08-21 Cognis Deutschland Gmbh Softening of polyolefin objects
NZ536482A (en) 2002-06-21 2007-03-30 Procter & Gamble Antimicrobial compositions, hygiene and personal care products and use thereof
US7998579B2 (en) * 2002-08-12 2011-08-16 Exxonmobil Chemical Patents Inc. Polypropylene based fibers and nonwovens
JP4311001B2 (en) 2002-11-28 2009-08-12 チッソ株式会社 Deodorant fiber and fiber molded product using the same
US20040116018A1 (en) * 2002-12-17 2004-06-17 Kimberly-Clark Worldwide, Inc. Method of making fibers, nonwoven fabrics, porous films and foams that include skin treatment additives
US8877316B2 (en) * 2002-12-20 2014-11-04 The Procter & Gamble Company Cloth-like personal care articles
US9018112B2 (en) * 2003-11-18 2015-04-28 Exxonmobil Chemicals Patents Inc. Extensible polypropylene-based nonwovens
CN100562612C (en) * 2006-04-26 2009-11-25 上海展扬纳米科技有限公司 A kind of antibiotic multifunctional fibre material and preparation method thereof
WO2009001871A1 (en) * 2007-06-26 2008-12-31 Idemitsu Kosan Co., Ltd. Elastic nonwoven fabric, process for producing the same, and textile product comprising the elastic nonwoven fabric
US20090053959A1 (en) * 2007-08-21 2009-02-26 Sudhin Datta Soft and Elastic Nonwoven Polypropylene Compositions
KR100903198B1 (en) * 2007-10-05 2009-06-18 코오롱글로텍주식회사 Polyolefin fiber and a method for preparation of the same
BRPI0906807B1 (en) * 2008-01-21 2019-02-19 Imerys Pigments, Inc. MONOFILING FIBER
KR100862331B1 (en) * 2008-05-13 2008-10-13 (주)유니맥스 Polypropylene multilayered absorbing fabric for medical use and manufacturing method thereof
MX2011010163A (en) * 2009-03-27 2011-10-10 3M Innovative Properties Co Hydrophilic polypropylene melt additives.
WO2011077592A1 (en) * 2009-12-25 2011-06-30 Sumitomo Chemical Company, Limited Polymer composition and molded articles shaped of the same
US20110224637A1 (en) * 2010-02-16 2011-09-15 Playtex Products, Llc LOW pH, OPTIMAL ORP, AND ODOR-REDUCING FIBERS, A PROCESS FOR MAKING THE FIBERS, AND ARTICLES MADE THEREFROM
KR20120111990A (en) * 2011-03-31 2012-10-11 유인식 The manufacturing method of the synthetic textiles included plant fatty acid
WO2012162130A1 (en) * 2011-05-20 2012-11-29 The Procter & Gamble Company Fibers of polymer-wax compositions

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0253950A (en) * 1988-08-12 1990-02-22 Kuraray Co Ltd Production of hydrophilic non woven fabric
JPH11323715A (en) * 1998-05-14 1999-11-26 Mitsui Chem Inc Top sheet material for absorptive article
JP2003500556A (en) * 1999-05-21 2003-01-07 スリーエム イノベイティブ プロパティズ カンパニー Hydrophilic polypropylene fiber with antibacterial activity
JP2002161428A (en) * 2000-11-29 2002-06-04 Nippon Supplement Kk METHOD FOR PRODUCING gamma-LINOLENIC ACID-CONTAINING FIBER
JP2008535955A (en) * 2005-03-14 2008-09-04 ロディア ルシェルシュ エ テクノロジー Composition comprising a thermoplastic polymer and a hydrophilizing agent
JP2010150674A (en) * 2008-12-24 2010-07-08 Mitsui Chemicals Inc Fiber and nonwoven fabric

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